Stephens R - Search Results

1

Reliability of high-throughput genotyping of whole genome amplified DNA in SNP genotyping studies.

Berthier-Schaad Y, Kao WH, Coresh J, Zhang L, Ingersoll RG, Stephens R, Smith MW. Berthier-Schaad Y, et al. Among authors: stephens r. Electrophoresis. 2007 Aug;28(16):2812-7. doi: 10.1002/elps.200600674. Electrophoresis. 2007. PMID: 17702060

2

Detecting AIDS restriction genes: from candidate genes to genome-wide association discovery.

Hutcheson HB, Lautenberger JA, Nelson GW, Pontius JU, Kessing BD, Winkler CA, Smith MW, Johnson R, Stephens R, Phair J, Goedert JJ, Donfield S, O'Brien SJ. Hutcheson HB, et al. Among authors: stephens r. Vaccine. 2008 Jun 6;26(24):2951-65. doi: 10.1016/j.vaccine.2007.12.054. Epub 2008 Feb 1. Vaccine. 2008. PMID: 18325640

3

Genome and gene alterations by insertions and deletions in the evolution of human and chimpanzee chromosome 22.

Volfovsky N, Oleksyk TK, Cruz KC, Truelove AL, Stephens RM, Smith MW. Volfovsky N, et al. BMC Genomics. 2009 Jan 26;10:51. doi: 10.1186/1471-2164-10-51. BMC Genomics. 2009. PMID: 19171065 Free PMC article.

4

An exhaustive DNA micro-satellite map of the human genome using high performance computing.

Collins JR, Stephens RM, Gold B, Long B, Dean M, Burt SK. Collins JR, et al. Among authors: stephens rm. Genomics. 2003 Jul;82(1):10-9. doi: 10.1016/s0888-7543(03)00076-4. Genomics. 2003. PMID: 12809672

5

Initial sequence and comparative analysis of the cat genome.

Pontius JU, Mullikin JC, Smith DR; Agencourt Sequencing Team; Lindblad-Toh K, Gnerre S, Clamp M, Chang J, Stephens R, Neelam B, Volfovsky N, Schäffer AA, Agarwala R, Narfström K, Murphy WJ, Giger U, Roca AL, Antunes A, Menotti-Raymond M, Yuhki N, Pecon-Slattery J, Johnson WE, Bourque G, Tesler G; NISC Comparative Sequencing Program; O'Brien SJ. Pontius JU, et al. Among authors: stephens r. Genome Res. 2007 Nov;17(11):1675-89. doi: 10.1101/gr.6380007. Genome Res. 2007. PMID: 17975172 Free PMC article.

6

Performance comparison of SNP detection tools with illumina exome sequencing data--an assessment using both family pedigree information and sample-matched SNP array data.

Yi M, Zhao Y, Jia L, He M, Kebebew E, Stephens RM. Yi M, et al. Nucleic Acids Res. 2014 Jul;42(12):e101. doi: 10.1093/nar/gku392. Epub 2014 May 15. Nucleic Acids Res. 2014. PMID: 24831545 Free PMC article.

7

Non-B DB: a database of predicted non-B DNA-forming motifs in mammalian genomes.

Cer RZ, Bruce KH, Mudunuri US, Yi M, Volfovsky N, Luke BT, Bacolla A, Collins JR, Stephens RM. Cer RZ, et al. Among authors: stephens rm. Nucleic Acids Res. 2011 Jan;39(Database issue):D383-91. doi: 10.1093/nar/gkq1170. Epub 2010 Nov 21. Nucleic Acids Res. 2011. PMID: 21097885 Free PMC article.

8

Mutation in CEP290 discovered for cat model of human retinal degeneration.

Menotti-Raymond M, David VA, Schäffer AA, Stephens R, Wells D, Kumar-Singh R, O'Brien SJ, Narfström K. Menotti-Raymond M, et al. Among authors: stephens r. J Hered. 2007 May-Jun;98(3):211-20. doi: 10.1093/jhered/esm019. Epub 2007 May 16. J Hered. 2007. PMID: 17507457

9

Sequences, annotation and single nucleotide polymorphism of the major histocompatibility complex in the domestic cat.

Yuhki N, Mullikin JC, Beck T, Stephens R, O'Brien SJ. Yuhki N, et al. Among authors: stephens r. PLoS One. 2008 Jul 16;3(7):e2674. doi: 10.1371/journal.pone.0002674. PLoS One. 2008. PMID: 18629345 Free PMC article.

10

AVIA: an interactive web-server for annotation, visualization and impact analysis of genomic variations.

Vuong H, Stephens RM, Volfovsky N. Vuong H, et al. Bioinformatics. 2014 Apr 1;30(7):1013-4. doi: 10.1093/bioinformatics/btt655. Epub 2013 Nov 9. Bioinformatics. 2014. PMID: 24215028 Free PMC article.

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